Electronic Supplementary Material (ESI) for CrystEngComm. This journal is © The Royal Society of Chemistry 2017 Electronic Supplementary Information for CrystEngComm This journal is (c) The Royal Society of Chemistry 2017 Electronic Supplementary Information (ESI) Effect of ligand configurations, secondary Pb-O interactions and auxiliary ligands on Pb(II)-mono/disulfonate complexes: synthesis, structures, and luminescent properties Guo-Zhen Huang, Xin Zou, Zhi-Biao Zhu, Zhao-Peng Deng,* Li-Hua Huo and Shan Gao* Electronic Supplementary Information for CrystEngComm This journal is (c) The Royal Society of Chemistry 2017 Fig. S1 3-D network of complex 1. Fig. S2 3-D supramolecular network of complex 2 extended by the C-H···O interactions. Electronic Supplementary Information for CrystEngComm This journal is (c) The Royal Society of Chemistry 2017 (a) (b) Fig. S3 Two types of layers in complex 3 extended by the C-H···O and π···π stacking interactions. Fig. S4 3-D supramolecular network of complex 5 extended by the O-H···O interactions. Electronic Supplementary Information for CrystEngComm This journal is (c) The Royal Society of Chemistry 2017 Fig. S5 3-D supramolecular network of complex 7 extended by π···π stacking interactions. Fig. S6 3-D supramolecular network of complex 8 extended by the O-H···N and π···π stacking interactions. The different π···π stacking interactions between two pyridyl rings, phenyl and pyridyl rings were denoted as different color. Electronic Supplementary Information for CrystEngComm This journal is (c) The Royal Society of Chemistry 2017 Fig. S7 TG curves of complexes 1-8 at N2 atmosphere. Electronic Supplementary Information for CrystEngComm This journal is (c) The Royal Society of Chemistry 2017 Fig. S8 PXRD patterns of complexes 1-8. Electronic Supplementary Information for CrystEngComm This journal is (c) The Royal Society of Chemistry 2017 Table S1 Selected Hydrogen Bond Parameters for Complexes 1-8a D-H...A d(D-H) d(H...A) d(D...A) <(DHA) Complex 1 O(1W)-H(1W1)...O(5)iii 0.85 2.09 2.754(11) 134.8 Complex 3 O(1W)-H(1W1)...O(2) 0.85 2.38 3.057(11) 137.1 Complex 4 O(1W)-H(1W1)...O(2)vii 0.85(9) 2.14(9) 2.889(13) 146(15) O(1W)-H(1W2)...N(1) 0.85(9) 2.01(11) 2.750(19) 145(18) Complex 5 O(1W)-H(1W1)...O(1)i 0.85(5) 1.99(5) 2.763(9) 151(10) O(1W)-H(1W1)...O(2)i 0.85(5) 2.59(8) 3.104(9) 120(8) O(1W)-H(1W2)...Cl(1)v 0.85(5) 2.73(5) 3.527(8) 155(10) O(2W)-H(2W1)...O(3W)ii 0.85(5) 1.858(16) 2.706(10) 174(9) O(2W)-H(2W2)...O(4)vi 0.85(5) 2.01(5) 2.798(9) 154(11) O(3W)-H(3W1)...O(4)ii 0.85(5) 2.22(9) 2.838(9) 130(9) O(3W)-H(3W2)...O(1)iv 0.85(5) 2.08(5) 2.846(11) 150(10) O(7)-H(7O)...O(3) 0.85(5) 1.83(4) 2.623(9) 155(10) Complex 6 O(1W)-H(1W1)...O(13)ii 0.85(4) 1.93(4) 2.773(13) 168(17) O(1W)-H(1W2)...O(3) 0.85(4) 2.31(11) 3.069(16) 149(20) Complex 7 O(1W)-H(1W1)...O(6W)ii 0.85 2.27 2.814(13) 121.4 O(1W)-H(1W2)...O(3)iii 0.85 2.22 2.899(11) 136.0 O(2W)-H(2W1)...O(5) 0.85 1.94 2.794(10) 179.8 O(2W)-H(2W2)...O(11) 0.85 1.91 2.762(10) 179.8 O(3W)-H(3W1)...O(2W)iv 0.85 2.24 3.093(15) 177.3 O(4W)-H(4W1)...O(9)i 0.85 1.90 2.749(12) 172.2 O(4W)-H(4W2)...O(6W) 0.85 2.48 3.328(18) 172.3 O(5W)-H(5W1)...O(13)i 0.85 2.26 3.101(15) 173.4 O(5W)-H(5W2)...O(2) 0.85 1.90 2.721(17) 162.7 O(6W)-H(6W1)...O(5W)i 0.85 2.14 2.93(2) 155.2 O(6W)-H(6W1)...O(13) 0.85 2.84 3.268(13) 112.8 O(7W)-H(7W2)...O(5) 0.85 2.36 2.91(2) 123.4 Complex 8 O(1W)-H(1W1)...O(4) 0.85 2.19 2.899(12) 140.3 O(1W)-H(1W1)...O(2W) 0.85 2.30 2.873(14) 125.0 O(1W)-H(1W2)...O(1)i 0.85 2.25 2.831(11) 125.3 O(1W)-H(1W2)...O(1)ii 0.85 2.39 3.097(13) 141.6 O(2W)-H(2W2)...N(2)iii 0.85 1.82 2.638(15) 159.8 O(7)-H(7O)...O(6) 0.85 2.43 2.944(9) 120.0 a Symmetry transformations used to generate equivalent atoms: iii -x,-y,-z+2 for 1; (vii) x,y,z+1 for 4; i x,-y+3/2,z-1/2, ii -x+1,y-1/2,-z+1/2, iii -x+1,y+1/2,-z+1/2, v x,-y+5/2,z-1/2, vi -x+2,y-1/2,-z+1/2 for 5; ii x-1,y,z for 6; i -x+1,-y,-z+1, ii x+1,y,z, iii -x+2,-y,-z+1, iv x-1,y,z for 7; i -x+2,-y,-z+1, ii x,y-1,z, iii x-1,y,z-1 for 8..